Canonical Allele Identifier: CA2275552437

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524030_75524031delinsGA , CM000679.2:g.75524030_75524031delinsGA	GRCh38
NC_000017.10:g.73520111_73520112delinsGA , CM000679.1:g.73520111_73520112delinsGA	GRCh37
NC_000017.9:g.71031706_71031707delinsGA	NCBI36
NG_013041.1:g.12503_12504delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1431-232_1431-231delinsGA MANE Select	ENSP00000327487.6:n.1431-232_1431-231delinsGA
ENST00000434205.8:c.1128-232_1128-231delinsGA	ENSP00000406559.4:n.1128-232_1128-231delinsGA
ENST00000545228.3:c.1619-232_1619-231delinsGA	ENSP00000438169.3:n.1619-232_1619-231delinsGA
ENST00000577197.2:n.629-232_629-231delinsGA
ENST00000579449.2:n.2171-232_2171-231delinsGA
ENST00000580013.6:n.2575-232_2575-231delinsGA
ENST00000679370.1:n.2953-232_2953-231delinsGA
ENST00000679429.1:c.*889-232_*889-231delinsGA	ENSP00000505403.1:n.*889-232_*889-231delinsGA
ENST00000679443.1:n.1500-232_1500-231delinsGA
ENST00000679782.1:c.*130-232_*130-231delinsGA	ENSP00000505995.1:n.*130-232_*130-231delinsGA
ENST00000679919.1:n.1702-232_1702-231delinsGA
ENST00000679928.1:c.*1983-232_*1983-231delinsGA	ENSP00000506071.1:n.*1983-232_*1983-231delinsGA
ENST00000680528.1:n.2397-232_2397-231delinsGA
ENST00000680999.1:c.1644-232_1644-231delinsGA	ENSP00000504984.1:n.1644-232_1644-231delinsGA
ENST00000681282.1:c.*1618-232_*1618-231delinsGA	ENSP00000506339.1:n.*1618-232_*1618-231delinsGA
ENST00000333213.10:c.1431-232_1431-231delinsGA	ENSP00000327487.6:n.1431-232_1431-231delinsGA
ENST00000545228.2:c.708-232_708-231delinsGA
ENST00000577197.1:n.179-232_179-231delinsGA
ENST00000579449.1:n.628-232_628-231delinsGA
NM_207346.2:c.1431-232_1431-231delinsGA	NP_997229.2:n.1431-232_1431-231delinsGA
XM_005257229.2:c.1619-232_1619-231delinsGA	XP_005257286.1:n.1619-232_1619-231delinsGA
XM_006721821.2:c.1316-232_1316-231delinsGA	XP_006721884.1:n.1316-232_1316-231delinsGA
XM_011524616.1:c.1502-232_1502-231delinsGA	XP_011522918.1:n.1502-232_1502-231delinsGA
XM_011524617.1:c.*13-232_*13-231delinsGA	XP_011522919.1:n.*13-232_*13-231delinsGA
XM_011524618.1:c.1314-232_1314-231delinsGA	XP_011522920.1:n.1314-232_1314-231delinsGA
XR_243646.2:n.1663-232_1663-231delinsGA
XM_005257229.4:c.1619-232_1619-231delinsGA	XP_005257286.1:n.1619-232_1619-231delinsGA
XR_001753015.1:n.87+280_87+281delinsTC
XR_001753016.1:n.88+280_88+281delinsTC
XR_243646.4:n.1669-232_1669-231delinsGA
NM_207346.3:c.1431-232_1431-231delinsGA MANE Select	NP_997229.2:n.1431-232_1431-231delinsGA